Thermoplastic Elastomer Composition Comprising An Elastomer, A Non-Elastomeric Polyolefin, And A Polyolefin Block Copolymer-Based Thermoplastic Elastomer

ABSTRACT

A thermoplastic elastomer composition of an elastomer, a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers are disclosed. Furthermore, the invention also relates to the use of a mixture of an elastomer and a cross-linking agent for the elastomer for producing a thermoplastic elastomer composition. A further subject of the invention is the use of a mixture of a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers for producing a thermoplastic elastomer composition. In addition, the invention relates to the use of a thermoplastic elastomer composition for producing a composite material with a polyolefin, in particular polypropylene. The invention also relates to a process for producing a thermoplastic elastomer composition as well as a composite material (article) made of the thermoplastic elastomer composition with a polyolefin.

The present invention relates to a thermoplastic elastomer composition of an elastomer, a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers. Furthermore, the present invention also relates to the use of a mixture of an elastomer and a cross-linking agent for the elastomer for producing a thermoplastic elastomer composition according to the invention. A further subject of the present invention is the use of a mixture of a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers for producing a thermoplastic elastomer composition according to the invention. In addition, the present invention relates to the use of a thermoplastic elastomer composition according to the invention for producing a composite material with a polyolefin. The present invention also relates to a process for producing a thermoplastic elastomer composition according to the invention as well as a composite material (article) made of the thermoplastic elastomer composition according to the invention with a polyolefin.

In the state of the art only thermoplastic elastomer compositions such as for example THERMOLAST® K, THERMOLAST® V, THERMOLAST® A and HIPEX® from Kraiburg TPE GmbH & Co. KG are known, which have either a good adhesion to thermoplasts, such as polyolefins, or a good chemical resistance. No thermoplastic elastomer compositions are known which have both a good adhesion to polyolefins, such as for example polypropylene, and a good chemical resistance. The latter applies in particular in the most required Shore A hardness range of from 30 to 90. By “chemical resistance” is meant, according to the invention, preferably a resistance to motor vehicle operating fluids, such as engine oils, transmission oils, fuels such as gasoline and diesel, as well as other operating fluids such as AdBlue® or coolants.

There is thus a requirement, in particular in the automotive sector as well as its plastics-processing supply industry, for thermoplastic elastomer compositions which have a good adhesion to polyolefins, preferably polypropylene, and a good chemical resistance.

The object of the present invention was therefore to provide a thermoplastic elastomer composition which has both a good adhesion to thermoplasts, such as polyolefins, e.g. polypropylene, and a good chemical resistance. In addition, the hardnesses of the thermoplastic elastomer compositions should lie in the range of from 30 to 90 Shore A (ShA).

The object according to the invention is achieved by the provision of a thermoplastic elastomer composition which contains an elastomer, a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers (TPO), wherein the elastomer comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber, silicone rubber, styrene butadiene rubber, chloroprene rubber, bromobutyl rubber, epichlorohydrin rubber, epoxidized natural rubber and a mixture of two or more of the named elastomers, wherein the elastomer can be present as cross-linked or non-cross-linked elastomer.

According to the present application, by a “thermoplastic elastomer” is meant a TPE which consists of a polymer or a polymer mixture (blend) and at its temperature of use has properties which are similar to those of vulcanized rubber which however, at raised temperatures, can be processed and worked up like a thermoplastic material. The same also applies to the thermoplastic elastomer compositions according to the invention.

In particular the present invention also relates to an embodiment in which, in the thermoplastic elastomer composition according to the invention, the elastomer preferably comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber and a mixture of two or more of the named elastomers, wherein the named elastomers can be present as cross-linked or non-cross-linked elastomers. It is particularly preferred that the elastomer comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber and a mixture of both elastomers, wherein the elastomers can be present as cross-linked or non-cross-linked elastomers.

It is further preferred that the elastomer in the composition according to the invention consists of one or more of the named elastomers.

The composition according to the invention can be present cross-linked or non-cross-linked, and can comprise a cross-linking agent or no cross-linking agent. There are in principle different states in which the thermoplastic elastomer composition according to the invention can be present:

a) the elastomer is present cross-linked and the thermoplastic elastomer composition according to the invention contains no further cross-linking agent;

b) the elastomer is present (partially) cross-linked and the thermoplastic elastomer composition according to the invention furthermore contains a cross-linking agent;

c) the elastomer is present non-cross-linked and the composition according to the invention contains a cross-linking agent;

d) the elastomer is present non-cross-linked and the composition preferably also contains no cross-linking agent.

In an embodiment of the present invention it is therefore preferred that the thermoplastic elastomer composition according to the invention additionally comprises a cross-linking agent.

In an alternative embodiment it is preferred that in the thermoplastic elastomer composition according to the invention the elastomer is present as cross-linked elastomer.

In a further embodiment of the present invention the thermoplastic elastomer composition according to the invention preferably comprises the TPO as block copolymer, which comprises or consists of at least two different alkylene units. By “alkylene units” is meant the repeat units of the polymer from which the polymer is formed by polymerization. It is here particularly preferred that the block copolymer comprises ethylene and propylene units or consists of these units.

In a preferred embodiment of the present invention the non-elastomeric polyolefin in the thermoplastic composition according to the invention is a polypropylene.

The cross-linking agents listed below—depending on the elastomer used—can be used as cross-linking agents in the thermoplastic elastomer composition according to the invention.

In the thermoplastic elastomer composition according to the invention, the weight ratio of elastomer to the non-elastomeric polyolefin preferably lies in the range of from 100:15 to 100:60, more preferably in the range of from 100:15 to 100:50.

It is further preferred that in the thermoplastic elastomer composition according to the invention the weight ratio of elastomer to TPO lies in the range of from 100:5 to 100:45, more preferably in the range of from 100:5 to 100:30.

The thermoplastic elastomer composition can in addition contain a plasticizer. Corresponding plasticizers which can be used according to the invention are also described below. The plasticizer is here preferably used in a weight ratio of elastomer to plasticizer in the range of from 100:40 to 100:15, more preferably in a range of from 100:30 to 100:20.

Furthermore, the thermoplastic elastomer composition according to the invention can also contain further additives such as a stabilizer, an auxiliary material, a dye, a filler and/or a compatibilizer. These are also described in more detail below.

A stabilizer, auxiliary material and/or dye is preferably used in each case in a weight ratio of elastomer to the named substances used in a range of from 100:4 to 100:0.01 and more preferably in a range of from 100:0.05 to 100:3. A filler is preferably used in a weight ratio of elastomer to filler in a range of from 100:100 to 100:1.

In addition to the cross-linking agent the thermoplastic elastomer composition according to the invention can also contain a co-crosslinker. Co-crosslinkers that can be used according to the invention are also described below.

The present invention also relates to the use of a mixture of an elastomer and a cross-linking agent for the elastomer for producing a thermoplastic elastomer composition according to the invention, wherein the elastomer is selected from the same group of elastomers which are named above in connection with the thermoplastic elastomer composition according to the invention. The elastomers mentioned as preferred are also preferred in the use according to the invention. The weight ratio of elastomer to cross-linking agent preferably also lies in the range indicated for the thermoplastic elastomer composition according to the invention.

The use of the mixture of an elastomer and a cross-linking agent for the elastomer according to the invention can additionally include a co-crosslinker, a plasticizer or a further additive. The co-crosslinkers, plasticizers or further additives also named above in connection with the thermoplastic elastomer composition according to the invention are also preferably used here. The weight ratios indicated in connection with the thermoplastic elastomer composition according to the invention are also preferred here.

The present invention furthermore relates to the use of a mixture of a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers (TPO) for producing an elastomer composition according to the invention. Thermoplastic elastomers based on polyolefin block copolymers as well as non-elastomeric polyolefins that can be used according to the invention are described below.

The present invention also relates to the use of a thermoplastic elastomer composition according to the invention for producing a composite material with a polyolefin, preferably a polypropylene, or for the adhesion of the thermoplastic elastomer composition according to the invention to a polyolefin. The non-elastomeric polyolefin in the thermoplastic elastomer composition according to the invention and the polyolefin with which a composite material is produced can be identical or different. In other words, the present invention also relates to a process for producing an article, e.g. in the form of a composite material, made of the thermoplastic elastomer composition according to the invention and a polyolefin, wherein the thermoplastic elastomer composition is combined with a polyolefin. In the use according to the invention or the process according to the invention, injection moulding, multi-component injection moulding, injection moulding around inserts, extrusion or compression moulding is used as processing method for producing the composite materials, wherein injection moulding, injection moulding around inserts, multi-component injection moulding and extrusion are preferred, and multi-component injection moulding is quite particularly preferred.

Thus the present invention also relates to an article, e.g. in the form of a composite material, made of a thermoplastic elastomer composition according to the invention and a polyolefin.

The present invention also relates to the use of a thermoplastic elastomer composition according to the invention for producing components or shaped bodies in automobile interiors as well as under the hood, i.e. in the engine space of vehicles, for producing industrial devices, industrial tools, bathroom fittings, domestic appliances, medical consumables and devices, containers for sanitary products and cosmetics and sealing materials in general.

Furthermore, the present invention also relates to a process for producing a thermoplastic elastomer composition according to the invention, wherein an elastomer is mixed with a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers (TPO), wherein the elastomer is selected from the group of elastomers which are indicated above in connection with the thermoplastic elastomer composition according to the invention. The elastomers indicated as preferred are also preferred here. The weight ratios indicated in the thermoplastic elastomer composition according to the invention are also the ratios in which the components are used in the process according to the invention. Preferred process details are also described below.

The components named above and used in the thermoplastic elastomer compositions according to the invention or the uses and processes according to the invention are described in more detail hereafter:

A: elastomer

B: non-elastomeric polyolefin

C: thermoplastic elastomer based on polyolefin block copolymers

D: cross-linking agent

E: co-crosslinker

F: plasticizer

G: stabilizer, auxiliary material, dye

H: filler

Component A: Elastomer

By the term “elastomer” is meant not only a single elastomer, but also a mixture of two or more elastomers. In all the embodiments according to the invention, the elastomer contains (or consists of) an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber, silicone rubber, styrene butadiene rubber, chloroprene rubber, bromobutyl rubber, epichlorohydrin rubber, epoxidized natural rubber or a mixture of the named elastomers. A single one of the named elastomers, but also a combination of two or more of the named elastomers can be used as elastomer. The elastomers can be present in the thermoplastic elastomer composition according to the invention in their non-cross-linked form, however they can also be present cross-linked. Descriptions of the individual classes of elastomer as well as commercially available products are to be found for example in Chapter 7.1. of “K. Oberbach, Kunststoff Taschenbuch [Plastics Handbook], Carl Hanser Verlag Munich Vienna, 26th edition (1995)”.

Ethylene-vinyl acetate copolymers (EVM) are copolymers of ethylene and vinyl acetate. EVMs are commercially available for example under the trade names Levapren® or Levamelt® from Lanxess Deutschland GmbH. Ethylene-vinyl acetate copolymers preferably used according to the invention are Levamelt® 400 (40±1.5 wt.-% vinyl acetate), Levamelt® 450 (45±1.5 wt.-% vinyl acetate), Levamelt® 452 (45±1.5 wt.-% vinyl acetate), Levamelt® 456 (45±1.5 wt.-% vinyl acetate), Levamelt® 500 (50±1.5 wt.-% vinyl acetate), Levamelt® 600 (60±1.5 wt.-% vinyl acetate), Levamelt® 700 (70±1.5 wt.-% vinyl acetate), Levamelt® 800 (80±2 wt.-% vinyl acetate) and Levamelt® 900 (90±2 wt.-% vinyl acetate), or the corresponding types of Levapren®, wherein Levamelt® 600 is particularly preferred. In the compositions according to the invention, an ethylene-vinyl acetate copolymer can be used as a component; however it is also possible to use mixtures of two or more ethylene-vinyl acetate copolymers. The cross-linking in the case of EVMs takes place peroxidically.

Nitrile butadiene rubber (NBR) are copolymers of acrylonitrile (ACN) and 1,3-butadiene with varying compositions. Due to the double bonds that they contain, NBRs can be cross-linked both peroxidically and by means of phenolic resins or sulphur. In the thermoplastic elastomer compositions according to the invention peroxidic cross-linking and cross-linking by means of phenolic resins are preferably used. Examples of NBRs to be used according to the invention are known by the trade names Perbunan®, Krynac®, Buna® N, or Europrene® N and are commercially available.

Hydrogenated nitrile butadiene rubber (H-NBR) is obtained by hydrogenation of the double bonds contained in NBR. H-NBR can be cross-linked peroxidically. Examples of H-NBR to be used according to the invention are known by the trade names Therban® (Lanxess) and Therban® AT (Lanxess) and are commercially available.

Butyl rubber (IIR) is also named isobutene-isoprene rubber. From the group of elastomers, IIR is one of the synthetic rubbers. IIR is a copolymer of isobutene and isoprene, wherein isobutene is preferably present in a quantity of from 95 to 99 mol.-% and isoprene in a quantity of from 1 to 5 mol.-%, relative to the total molecular weight. It is preferably cross-linked according to the invention phenolically or using peroxides.

Natural rubber (NR) is a homopolymer of isoprene which comprises almost exclusively 1,4-cis linking. Typically, the average molecular weight Mw is approximately 2*10⁶ g/mol. NR is preferably cross-linked according to the invention phenolically or using peroxides.

Isoprene rubber (IR) is the synthetically produced variant of natural rubber. It differs from the latter primarily due to its somewhat lower chemical purity. This is due to the fact that the catalysts used for the polymerization have a lower effectiveness than the enzymes occurring in nature. The purity of natural rubber is preferably more than 99.9%, whereas in the case of synthetically produced IR—depending on the catalyst used—only approximately 92% to 97% is achieved. Like natural rubber, IR can also be cross-linked peroxidically, phenolically or with sulphur. The cross-linking preferably takes place phenolically or using peroxides.

Acrylate rubbers (ACM) are copolymers of acrylic acid alkyl esters and a further vinylic polymer, such as for example a copolymer of acrylic acid ester and 2-chloroethyl vinyl ether or a copolymer of acrylic acid ester and acrylonitrile. The nature of the cross-linking of such polymers is dependent on the comonomers used.

Ethylene acrylate rubber (AEM) is a copolymer of ethylene and methyl acrylate. The latter is commercially available for example as Vamac® from DuPont.

Silicone rubbers are produced from convertible materials in the rubbery-elastic state, which contain poly(organo)siloxanes and which comprise groups accessible for cross-linking reactions. In other words, silicone rubbers are poly(organo)siloxanes which are cross-linked with a cross-linking agent. The cross-linking can take place by means of (organic) peroxides; it can however also result in that Si—H groups are catalytically added to silicon-bound vinyl groups, wherein both groups are incorporated into the polymer chains or at the ends thereof.

Styrene butadiene rubber (SBR) is a copolymer of styrene and 1,3-butadiene, wherein according to the invention the styrene content should be below 25% (in relation to the butadiene content), as the rubber takes on thermoplastic properties in the case of a higher styrene content. SBR can be cross-linked both peroxidically and by means of phenolic resins as well as by means of sulphur. In the compositions according to the invention peroxidic cross-linking and cross-linking by means of phenolic resins are preferably used here. Examples of SBR to be used according to the invention are known by the trade names Kralex® and Europrene® SBR and are commercially available.

Chloroprene rubber (CR) is also named polychloroprene or chlorobutadiene rubber and is a synthetic rubber which is also known by the trade name Neopren®. Neopren® is a trade name of the company DuPont, the trade name of Lanxess is e.g. Baypren®. Production takes place by polymerization of 2-chloro-1,3-butadiene (chloroprene).

Bromobutyl rubber (brominated IRR) is butyl rubber which is halogenated with bromine. For this, the rubber is preferably dissolved in an inert solvent and liquid bromine is added under vigorous stirring. The resulting hydrogen bromide is neutralized with sodium hydroxide solution.

Epichlorohydrin rubber (ECO) is produced by ring-opening polymerization of epichlorohydrin optionally in the presence of further comonomers. Epichlorohydrin rubber is commercially available for example under the trade name HydrinECO® from Zeon.

By “epoxidized natural rubber” is meant natural rubber as defined above, which has been epoxidized.

Component B: Non-Elastomeric Polyolefin

Non-elastomeric polyolefins are for example copolymers of polyethylene, such as HDPE (high density polyethylene), MDPE (medium density polyethylene), LDPE (low density polyethylene), LLDPE (linear low density polyethylene), VLDPE (very low density polyethylene); a homopolymer of propylene; a random copolymer of propylene and ethylene; and combinations thereof.

Polyolefins suitable for the invention are above all those which are suitable for processing in injection moulding. Suitable polyolefins are those with good flow properties and rigidity.

Homopolymers of propylene (hPP) are commercially available and each of these available hPPs can be used according to the invention.

The hPP can have a melt flow index value according to ISO 1133 (at 230° C. with 2.16 kg) in the range of from 0.5 g/10 min to 200 g/10 min, and preferably in the range of from 4 g/10 min to 50 g/10 min; a tensile strength according to ISO 527-1, −2 in the range of from 15 MPa to 50 MPa, and preferably in the range of from 20 MPa to 40 MPa; an elongation at break according to ISO 527-1, −2 in the range of from 1% to 500%, and preferably in the range of from 10% to 300%.

Commercially available hPPs are for example products from Lyondell-Basell, which are available under the trade name Moplen®, such as Moplen® HP500N and Moplen® HP501L.

Random polypropylene copolymers (rPP) are also commercially available and each of these rPPs can be used according to the invention. Ethylene and/or butene are preferred as comonomers.

The rPP can have a melt flow index according to ISO 1133 (at 230° C. with 2.16 kg) in the range of from 0.5 g/10 min to 200 g/10 min, and preferably in the range of from 4 g/10 min to 50 g/10 min; a tensile strength according to ISO 527-1, −2 in the range of from 15 MPa to 50 MPa, and preferably in the range of from 20 MPa to 40 MPa; an elongation at break according to ISO 527-1, −2 in the range of from 1% to 500%, and preferably in the range of from 10% to 300%.

Polyethylenes of different densities can be used according to the invention. These are sufficiently commercially available.

Any polyethylene can be used, the melt flow of which is in the range of from 0.5 g/min to 10 g/10 min. HDPE can have a melt flow index according to ISO 1133 (at 190° C. with 2.16 kg) in the range of from 0.02 g/10 min to 55 g/10 min, and preferably in the range of from 0.9 g/10 min to 10 g/10 min; a tensile strength according to ISO 527-1, −2 in the range of from 12 MPa to 32 MPa, and preferably in the range of from 20 MPa to 30 MPa; an elongation at break according to ISO 527-1, −2 in the range of from 50% to 1200%, and preferably in the range of from 600% to 700%.

LDPE can have a melt flow index according to ISO 1133 (at 190° C. with 2.16 kg) in the range of from 0.5 g/10 min to 200 g/10 min, and preferably in the range of from 0.7 g/10 min to 7 g/10 min; a tensile strength according to ISO 527-1, −2 in the range of from 6 MPa to 33 MPa, and preferably in the range of from 12 MPa to 24 MPa; an elongation at break according to ISO in the range of from 100% to 800%, and preferably in the range of from 500% to 750%.

However, it is particularly preferred according to the invention that the non-elastomeric polyolefin is one which comprises propylene in its repeat units. Even more preferably, the non-elastomeric polyolefin is an hPP.

Component C: Thermoplastic Elastomer Based on Polyolefin Block Copolymers (TPO)

As TPOs based on polyolefin block copolymers according to the invention, those in Chapter 5 of “G. Holden, H. R. Kricheldorf, R. P. Quirk (Eds)., Thermoplastic Elastomers, Carl Hanser Verlag, third edition, Munich (2004)” can be used, wherein among the TPOs described therein, only the block copolymers (Chapter 5.1. and Chapter 5.3) are relevant to the present invention. TPOs based on blends such as for example EPDM and PP are not included in the TPOs according to the invention. The TPOs based on polyolefin block copolymers according to the invention are consequently block copolymers, the blocks of which are constructed from olefin monomers as repeat units. The TPOs based on polyolefin block copolymers according to the invention have at least two different polymer blocks. These blocks can be constructed from one type of olefin or from two or more types of olefin. The olefins used for constructing the TPOs based on polyolefin block copolymers according to the invention are aliphatic olefins such as e.g. ethylene, propylene or butylene, wherein ethylene and propylene are preferred according to the invention. Particularly preferably, the TPOs based on polyolefin block copolymers according to the invention are constructed exclusively from aliphatic olefins as so-called repeat units. According to the invention, the definition of the “TPOs based on polyolefin block copolymers” excludes those that have an aromatic radical (which are known to a person skilled in the art as TPSs (thermoplastic elastomers based on styrene)). TPOs, the blocks of which are constructed from or consist of polypropylene, polyethylene or a random ethylene/propylene copolymer, are particularly preferred for the application described here or the composition according to the invention. Such TPOs are commercially available for example under the trade name Hifax CA 10 A from LyondellBasell. Furthermore, the polyolefin block copolymers described in detail in U.S. Pat. No. 8,481,637 B2 (denoted there as “olefin block copolymers, OBCs”), which are referred to here in their entirety, are particularly preferred. These are polymers which have alternating blocks of a hard (very rigid) and a soft (highly elastomeric) segment. Such products are marketed by Dow Chemicals under the trade name INFUSE™. In particular the types recommended for use for TPEs are preferred (INFUSE™ 9010, 9007, 9107, 9807).

Further examples of TPOs based on polyolefin block copolymers according to the invention are so-called hydrogenated diene block copolymers. Such polymers preferably have polymer blocks which consist of hydrogenated polybutadiene or hydrogenated polyisoprene.

Component D: Cross-Linking Agent

Depending on the elastomer used, it is known to a person skilled in the art, which cross-linking agent can be used in order to achieve a cross-linking. According to the invention the elastomers named above can be cross-linked either by the addition of peroxides, phenolic resins, sulphur or metal ions.

Peroxides suitable as radical cross-linking initiators (cross-linking agents) are known to a person skilled in the art. Examples of these are organic peroxides, e.g. alkyl and aryl peroxides, alkyl peracid ester, aryl peracid ester, diacyl peroxides, polyvalent peroxides such as 2,5-dimethyl-2,5-di(tert-butylperoxy)hexyne-3 (e.g. Trigonox® 145-E85 or Trigonox® 145-45 B), di-tert-butyl peroxide (e.g. Trigonox® B), 2,5-dimethyl-2,5-di(tert-butylperoxy)hexyne (e.g. Trigonox® 101), tert-butyl-cumyl peroxide (e.g. Trigonox® T), di-tert-butyl-peroxyisopropyl(benzene) (e.g. Perkadox® 14-40), dicumyl peroxide (e.g. Perkadox® BC40), benzoyl peroxide, 2,2-bis (tert-butylperoxy)diisopropylbenzene (e.g. Volcup® 40 AE), 3,2,5-trimethyl-2,5-di(benzoylperoxy)hexane and (2,5-bis(tert-butylperoxy)-2,5-dimethylhexane, 3,3,5,7,7-pentamethyl-1,2,4-trioxepane (e.g. Trigonox® 311).

Peroxides the cross-linking temperatures of which are above the melting or softening temperatures of component A are preferably used. Because of the high melting or softening temperature of component B, according to the invention the cross-linking of the elastomeric phase (of the elastomer) for producing the thermoplastic elastomer compositions preferably takes place in a correspondingly hot melt. This requires—in a preferred embodiment—the use of peroxides with high cross-linking temperatures. Peroxides with lower (usual) cross-linking temperatures already decompose on first contact with the polymer melt and are not mixed in homogeneously and cross-link the elastomeric phase insufficiently or inhomogeneously. Therefore peroxides are particularly preferably used according to the invention, which have cross-linking temperatures of ≧175° C., particularly preferably ≧180° C., quite particularly preferably ≧185° C., especially preferably ≧190° C. and further preferably ≧200° C.

When a peroxide is used as cross-linking agent it is furthermore preferred according to the invention that the (still cross-linkable) thermoplastic elastomer compositions have a weight ratio of peroxide to elastomer in a range of from 0.1 to 5, preferably 0.5 to 5, and quite particularly preferably 0.6 to 1.8.

In particular when diene-containing rubbers, such as e.g. NBR, are used as component A, in addition to peroxidic cross-linking phenolic resins are also suitable for cross-linking component A. Here phenolic resins with sufficiently high reactivity at mixing temperatures of at least 220° C. are preferably used. Brominated phenolic resins are also to be named here.

To accelerate the phenolic resin cross-linking inorganic compounds known to a person skilled in the art are used. For example SnCl₂ and/or ZnO and/or ZnCl₂ can be used for acceleration and catalysis of the reaction. However, halogen-containing elastomers can also be used. ZnO is particularly preferably used as it also acts as catalyst.

In the case of non-brominated phenolic resins, it is also useful to add halogen donors in the form of Lewis acids or chloroprene rubber. Thus in the thermoplastic elastomer compositions according to the present invention a combination of at least one phenolic resin and at least one Cl-containing Lewis acid, preferably SnCl₂, can be used as cross-linking agent. ZnCl₂ or SnCl₂ is preferably used as Cl-containing Lewis acid, wherein it is preferred that ZnO is additionally used when SnCl₂ is used. As an alternative to the named Lewis acids a mixture of chloroprene rubber and ZnO can also be used. In the case of the use of brominated phenolic resins the use of a Lewis acid is preferably not necessary; however ZnO is then preferably additionally used. Phenolic resins suitable for this purpose are known to a person skilled in the art and are usually obtained by reaction of phenol with aldehydes (phenol-formaldehyde resin). Phenolic resins suitable for this purpose are for example the products of the reaction of octylphenol with formaldehyde, e.g. SP-1045 H (SP-1045, HRJ-10518 H from Schenectady International Inc.), which is an octylphenol-formaldehyde resin that contains methylol groups, is suitable, or in the case of brominated phenolic resins, brominated octylphenol resins, for example those with the trade names SP-1055 or SP-1056. Suitable Cl-containing Lewis acids are known to a person skilled in the art. SnCl₂ or chloroprene rubber is preferably used.

When the combination of at least one phenolic resin with at least one Cl-containing Lewis acid, preferably SnCl₂, is used, the at least one phenolic resin is preferably used in a quantity of from 2 to 5 wt.-%, relative to the total weight of the thermoplastic elastomer composition, and the Cl-containing Lewis acid is preferably used in a quantity of from 0.2 to 0.7 wt.-%, relative to the total weight of the thermoplastic elastomer composition.

Cross-linking using sulphur is one of the oldest possibilities for cross-linking rubbers, which is known to a person skilled in the art in this field.

Component E: Co-Crosslinker

In a preferred embodiment according to the invention, the thermoplastic elastomer compositions additionally contain at least one co-crosslinker as component E. The co-crosslinker is according to the invention preferably used in a weight ratio of elastomer to co-crosslinker in the range of from 100:10 to 100:2 and more preferably in the range of from 100:8 to 100:3.

Suitable co-crosslinkers for peroxides as cross-linking agents are for example from the group consisting of triallyl isocyanurate (TAIL) (e.g. DIAK™-7 from DuPont), trimethylolpropane trimethacrylate (TRIM) (e.g. Rhenogran® TRIM S from Rheinchemie), N,N′-m-phenylene dimaleimide (e.g. HVA™-2 from DuPont Dow), triallyl cyanurate (TAC), liquid polybutadiene (e.g. Ricon® D153 from Ricon Resins), p-quinone dioxime, p,p′-dibenzoyl quinone dioxime, N-methyl-N,N-dinitrosoaniline, nitrobenzene, diphenylguanidine, trimethylolpropane-N,N′-m-phenylene maleimide, N-methyl-N,N′-m-phenylene dimaleimide, divinylbenzene, polyfunctional methacrylate monomers such as ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, polyethylene glycol dimethacrylate, trimethylolpropane trimethacrylate and allyl methacrylate, and polyfunctional vinyl monomers such as vinyl butyrate and vinyl stearate. Preferably used co-crosslinkers are selected from the group consisting of trimethylolpropane trimethacrylate (TRIM), triallyl isocyanurate (TAIL), N,N′-m-phenylene dimaleimide, triallyl cyanurate (TAC) and liquid polybutadiene. Trimethylolpropane trimethacrylate (TRIM) is particularly preferably used as co-crosslinker. It is possible, in the cross-linkable compositions according to the invention, to use one co-crosslinker or two or more co-crosslinkers jointly.

Component F: Plasticizer

Suitable plasticizers are in principle known to a person skilled in the art. Suitable plasticizers for polar elastomers (EVM, NBR, H-NBR, AEM, ACM, etc.) are e.g. ester plasticizers such as phthalic acid esters, for example dioctyl phthalate, diisooctyl phthalate, dinonyl phthalate or diisodecyl phthalate; aliphatic esters such as dioctyl acid ester or dioctyl sebacic acid ester; phosphoric acid esters such as tricresyl phosphoric acid ester, diphenyl cresylic acid ester or trioctyl phosphate; polyesters such as polyphthalic acid ester, polyadipic acid ester or polyester ether.

Suitable plasticizers for non-polar elastomers (e.g. styrene butadiene rubber) are technical or medical mineral or white oils, native oils such as for example soya or rapeseed oil, also alkylsulphonyl ester, in particular alkylsulphonyl phenyl ester, wherein the alkyl substituents contain linear and/or branched alkyl chains with >5 C atoms. Also, di- or trialkyl esters of mellitic acid, wherein the alkyl substituents preferably contain linear and/or branched alkyl chains with >4 C atoms. Furthermore, alkyl esters of di-, tri- and higher polycarboxylic acids, wherein the alkyl substituents are preferably linear and/or branched alkyl chains, are also used as corresponding plasticizers. The following may be named as examples: di-2-ethylhexyl adipate and tributyl O-acetylcitrate. Furthermore, carboxylic acid esters of mono- and/or polyalkylene glycols can also be used as plasticizers, such as for example ethylene glycol adipate.

Mixtures of the substance classes described can also be used as suitable plasticizers.

Component G: Stabilizers, Auxiliary Materials and Dyes (Additives)

Suitable additives are e.g. processing auxiliary materials, metal soaps, fatty acids and fatty acid derivatives, factice ([made-up word]: rubber-like substance which is obtained e.g. by the action of sulphur or sulphur chloride on drying oils; serves for stretching rubber), anti-ageing agents, anti-UV agents or antiozonants such as antiozonant waxes, antioxidants, e.g. polycarbodiimides (e.g. Rhenogran®, PCD-50), substituted phenols, substituted bisphenols, dihydroquinolines, diphenylamines, phenylnaphthylamines, paraphenylenediamines, benzimidazoles, paraffin waxes, microcrystalline waxes, pigments, dyes such as titanium dioxide, lithopone, zinc oxide, iron oxide, ultramarine blue, chromium oxide, antimony sulphite; stabilizers such as heat stabilizers, stabilizers against weathering; means of protection against oxidation, e.g. p-dicumyldiphenylamine (e.g. Naugare® 445), styrenated diphenylamine (e.g. Vulcanox® DDA), zinc salt of methyl mercaptobenzimidazole (e.g. Vulcanox® ZMB2), polymerized 1,2-dihydro-2,2,4-trimethylquinoline (e.g. Vulcanox® HS), thiodiethylene bis(3,5-di-tert-butyl-4-hydroxy)hydrocinnamate, thiodiethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] (e.g. Irganox® 1035), lubricants, release agents, flame retardants (fire protection agents), adhesion promoters, tracers, minerals as well as crystallization accelerators and retarders.

The following can be used as processing auxiliary materials and stabilizers: antistatics, anti-foaming agents, lubricants, dispersants, release agents, anti-blocking agents, free-radical scavengers, antioxidants, biocides, fungicides, UV stabilizers, other light stabilizers, metal deactivators, furthermore also additives such as foaming aids, propellants, fire protection agents, flue gas suppressors, impact resistance modifiers, adhesive agents, anti-fogging agents, dyes, colour pigments, colour masterbatches, viscosity modifiers and means for protection against ageing.

Stabilizers and anti-ageing agents are particularly preferably used as auxiliary materials.

Component H: Fillers

Suitable fillers are e.g. soot, chalk (calcium carbonate), kaolin, siliceous earth, talc (magnesium silicate), aluminium oxide hydrate, aluminium silicate, calcium carbonate, magnesium carbonate, calcium silicate, magnesium silicate, barium sulphate, zinc carbonate, calcined kaolin (e.g. Polestar® 200 P), calcium oxide, magnesium oxide, titanium oxide, aluminium oxide, zinc oxide, silanized kaolins, silanized silicate, coated chalk, treated kaolins, fumed silica, hydrophobic fumed silica (e.g. Aerosil® 972), synthetic amorphous precipitated silica, carbon black, graphite, nanoscale fillers such as carbon nanofibrils, nanoparticles in platelet form or nanoscale silicon dioxide hydrates and minerals.

Production of the compositions according to the invention and cross-linking or mixing to form thermoplastic elastomer compositions:

The thermoplastic elastomer compositions according to the present invention can be produced by mixing components A, B, C, D, E, F, G and H—insofar as they are present in the compositions. Mixing can take place using mixing systems known in rubber technology and plastic technology such as kneaders, internal mixers, e.g. internal mixers with intermeshing or tangential rotor geometry, as well as also in continuous mixing equipment such as mixing extruders, e.g. mixing extruders with 2 to 4 or more shaft screws (e.g. twin-screw extruders).

When carrying out the production process according to the invention it is important to ensure that the mixing temperature is sufficiently high that components B and C can be transformed into the plastic state, but are not damaged in the process. This is guaranteed if a temperature above the highest melting or softening temperature of components B and C is selected. The components—insofar as they are present in the compositions—are particularly preferably mixed at a temperature in the range of from 150° C. to 350° C., preferably 150° C. to 280° C., particularly preferably 170° C. to 240° C.

Different variants are in principle possible for mixing the individual components.

Variant 1: A, B, C, D, E, F, G and H—insofar as they are contained in the composition according to the invention—are provided jointly and intimately mixed at temperatures above the highest melting or softening temperatures of components B and C.

Variant 2: A, B, C, F, G and H—insofar as they are contained in the composition according to the invention—are provided jointly and intimately mixed at temperatures above the highest melting or softening temperatures of components B and C. Components D and E (insofar as they are present in the formulation according to the invention) are then added and further mixed on arriving at the temperature reached.

Variant 3: A, D, E, F, G and H—insofar as they are contained in the composition according to the invention—are provided jointly and intimately mixed until below the reaction temperature of D. Components B and C are then added and heated to the softening temperature of B and C with continuous mixing. The addition of B and C can take place above or below the softening temperature of B and C.

Variant 4: B, C and H—insofar as they are contained in the composition according to the invention—are provided jointly and intimately mixed at temperatures above the highest melting or softening temperatures of components B and C. Components A, D, E, F and G (insofar as they are contained in the formulation according to the invention) are added and further intimately mixed above the highest melting or softening temperatures of components B and C.

Variant 1 is particularly preferred for production in an internal mixer. Variant 3 is particularly preferred for production in continuous mixing equipment.

By means of the above-named process variants, in particular by means of process variants 1 and 3, it is achieved that component A and components B and C have undergone the finest and most homogeneous distribution possible after completion of production.

The addition time, temperature, form and quantity of components D and E should in addition be selected such that a good distribution of components D and optionally E in the elastomer phase is guaranteed, the elastomer and thermoplast phases (B, C) are present in the state described above and only then does the cross-linking of the elastomer phase take place, with the result that a phase reversal takes place or a co-continuous phase structure of the elastomeric phase and the thermoplastic phase takes place.

In the process according to the invention it is preferred that according to the indicated variant 3, the elastomer is blended with a mixture of a polypropylene and a thermoplastic elastomer based on polyolefin block copolymers (TPO) in an extruder, an internal mixer or a kneader, preferably in a twin-screw extruder.

In the process according to the invention of variant 3, the elastomer is preferably first pre-treated in a first process step, and a mixture of non-elastomeric polyolefin and TPO is added in a second process step.

In the first step it is preferred that the elastomer is pre-treated in an extruder, an internal mixer or a kneader, preferably in a twin-screw extruder. By “pre-treating” is preferably meant that the elastomer is softened, preferably at a temperature in the range of from 50° C. to 120° C., more preferably in the range of from 80° C. to 110° C. This pre-treatment preferably takes place in one of the devices indicated. This procedure is known to a person skilled in the art by the term “mastication”. A cross-linking agent is preferably used in addition to the elastomer, with the result that the softened elastomer is mixed together with a cross-linking agent. In addition to the elastomer and the cross-linking agent, a co-crosslinker, a plasticizer or one of the additives indicated above can also be added. The cross-linking agent, the co-crosslinker, the plasticizer or the further additives are preferably those named above in connection with the thermoplastic elastomer composition according to the invention.

Furthermore, it is preferred that in the process according to the invention preferably according to variant 3 before the second step, i.e. preferably in parallel with the first process step, the mixture of a non-elastomeric polyolefin and TPO is produced. This mixture is preferably also produced in an extruder, an internal mixer or a kneader, preferably in a twin-screw extruder. It is preferred that the mixture of the non-elastomeric polyolefin and TPO is produced at a temperature in the range of from 160° C. to 280° C., more preferably 200° C. to 260° C.

As already mentioned, after the second process step, i.e. the addition of the mixture of the non-elastomeric polyolefin and TPO to the elastomer, the resulting composition is blended. In other words, in a third process step, the batch comprising elastomer and the mixture of non-elastomeric polyolefin and TPO as well as optional further components is preferably extruded, more preferably at a temperature in the range of from 180° C. to 260° C., more preferably in a range of from 200° C. to 240° C. Kneading of the batch obtained in the third process step preferably takes place in a fourth process step.

The compositions according to the invention are outstandingly suitable for providing thermoplastic elastomers with balanced properties, in particular with very good temperature and chemical resistance with simultaneously very good elastic properties (compression set, elongation at break and tensile strength) in a broad hardness range. In addition they exhibit an excellent adhesion to polyolefins (in particular polypropylenes).

According to the present invention it is preferred that the elastomer is cross-linked during or after blending with the mixture of non-elastomeric polyolefin and TPO, i.e. the cross-linking takes place dynamically. The cross-linking of the preferably dispersed elastomeric phase (elastomer) preferably takes place during the mixing of components A to H (insofar as these are present in the mixture). The cross-linking preferably starts when the blending is continued at a temperature above the melting or softening temperature of components B and C in the presence of components D and optionally E over a period of at least 15 sec.

After phase reversal or formation of a co-continuous phase has taken place, the product obtained, i.e. the thermoplastic elastomer composition, is cooled down preferably to a temperature below the melting or softening temperature of component(s) B and/or C.

A further subject of the present invention is thermoplastic elastomer compositions which can be obtained by the processes according to the invention.

The terms “comprise”, “contain” and “have” used in the present application are meant in each case where they are used to also cover the term “consist of”, with the result that these embodiments are also disclosed in this application.

Furthermore, the present invention also relates to the following aspects:

A first aspect relates to a thermoplastic elastomer composition which contains an elastomer, a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers (TPO), wherein the elastomer comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber, silicone rubber, styrene butadiene rubber, chloroprene rubber, bromobutyl rubber, epichlorohydrin rubber, epoxidized natural rubber and a mixture of two or more of the named elastomers, wherein the elastomer can be present as cross-linked or non-cross-linked elastomer.

A second aspect relates to the thermoplastic elastomer composition according to aspect 1, wherein the elastomer comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber and a mixture of the named elastomers.

A third aspect relates to the thermoplastic elastomer composition according to aspect 1 or 2, which additionally comprises a cross-linking agent.

A fourth aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 3, wherein the elastomer is present as cross-linked elastomer.

A fifth aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 4, wherein a mixture of the non-elastomeric polyolefin and the TPO represents the matrix into which the elastomer is incorporated.

A sixth aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 5, wherein the TPO is a block copolymer which comprises at least two different alkylene units.

A seventh aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 6, wherein the weight ratio of elastomer to non-elastomeric polyolefin lies in the range of from 100:15 to 100:60.

An eighth aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 7, wherein the weight ratio of elastomer to TPO lies in the range of from 100:5 to 100:45.

A ninth aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 8, wherein the ratio of the weight of the elastomer to the sum of the weights of non-elastomeric polyolefin and TPO lies in the range of from 100:25 to 100:65.

A tenth aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 9, which additionally contains a plasticizer.

An eleventh aspect relates to the thermoplastic elastomer composition according to one of aspects 1 to 10, which additionally contains further additives.

A twelfth aspect relates to the use of a mixture of an elastomer and a cross-linking agent for the elastomer for producing a thermoplastic elastomer composition according to one of aspects 1 to 11, wherein the elastomer comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber, silicone rubber, styrene butadiene rubber, chloroprene rubber, bromobutyl rubber, epichlorohydrin rubber, epoxidized natural rubber and a mixture of two or more of the named elastomers.

A 13th aspect relates to the use according to aspect 12, wherein the mixture can contain a co-crosslinker, a plasticizer or a further additive.

A 14th aspect relates to the use of a mixture of a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers (TPO) for producing a thermoplastic elastomer composition according to one of aspects 1 to 11.

A 15th aspect relates to the use of a thermoplastic elastomer composition according to one of aspects 1 to 11 for producing a composite material with polyolefin, preferably a polypropylene.

A 16th aspect relates to a composite material made of a thermoplastic elastomer according to one of aspects 1 to 11 and a polyolefin.

A 17th aspect relates to the use of a thermoplastic elastomer composition according to one of aspects 1 to 11 for producing components or shaped bodies in automobile interiors as well as under the hood, i.e. in the engine space of vehicles, for producing industrial devices, industrial tools, bathroom fittings, domestic appliances, consumer electronics devices, sporting goods, medical consumables and devices, containers for sanitary products and cosmetics and sealing materials in general.

An 18th aspect relates to a process for producing a thermoplastic elastomer composition according to one of aspects 1 to 11, wherein an elastomer, a non-elastomeric polyolefin and a thermoplastic elastomer based on polyolefin block copolymers (TPO) are mixed, wherein the elastomer comprises an elastomer which is selected from the group of elastomers which consists of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber, silicone rubber, styrene butadiene rubber, chloroprene rubber, bromobutyl rubber, epichlorohydrin rubber, epoxidized natural rubber and a mixture of two or more of the named elastomers.

A 19th aspect relates to the process according to aspect 18, wherein the elastomer is mixed with a mixture of the non-elastomeric polyolefin and the thermoplastic elastomer based on polyolefin block copolymers (TPO) in an extruder, an internal mixer or a kneader, preferably in a twin-screw extruder.

A 20th aspect relates to the process according to aspect 19, wherein in a first step the elastomer is pre-treated and in a second step the mixture of non-elastomeric polyolefin and TPO is added.

A 21st aspect relates to the process according to aspect 19 or 20, wherein in the first step the elastomer softened by means of the temperature effect or the masticated elastomer is further mixed or masticated together with a cross-linking agent.

A 22nd aspect relates to the process according to one of aspects 19 to 21, wherein before the second step the mixture of non-elastomeric polyolefin and TPO is produced in an extruder, an internal mixer or a kneader, preferably in a twin-screw extruder.

A 23rd aspect relates to the process according to aspect 21 or 22, wherein in the first step the elastomer is mixed with the cross-linking agent in a temperature range of from 50° C. to 120° C.

A 24th aspect relates to the process according to aspect 22 or 23, wherein the mixture of non-elastomeric polyolefin and TPO is produced at a temperature in the range of from 160° C. to 280° C.

A 25th aspect relates to the process according to one of aspects 19 to 24, wherein in a third step the batch comprising elastomer and the mixture of non-elastomeric polyolefin and TPO as well as optional further components is extruded at a temperature in the range of from 180° C. to 260° C.

A 26th aspect relates to the process according to aspect 25, wherein the batch from the third step is kneaded.

The present invention will now be explained in more detail by means of the following embodiment examples. The following embodiment examples are only exemplary in nature and do not serve to limit the present invention thereto.

EXAMPLES

Methods of Determination and Definitions:

Determination of the density takes place according to DIN EN ISO 1183-1.

Determination of the Shore hardness takes place according to DIN EN ISO 868 and DIN ISO 7619-1.

By “tensile strength” is meant the maximum mechanical tensile stress which a material withstands before it breaks/tears. In the tensile test it is calculated from the maximum tensile force relative to the original cross section of the (standardized) sample and indicated in N/mm².

The elongation at break is a material characteristic which indicates the permanent lengthening in the case of the break, relative to the initial measurement length. In material testing, elongation at break is one of many parameters and characterizes the deformation capability of a material. It is the permanent change in length ΔL relative to the initial measurement length L₀ of a sample in the tensile test after breaking. This change in length is indicated in %.

The compression set is a measure of how (thermoplastic) elastomers behave in the case of long-lasting, constant compression and subsequent decompression. According to DIN ISO 815 the compression set (CS) is measured at constant strain. This represents the deformation component of the test material. Many test methods for elastomers, such as e.g. tensile strength, characterize the quality and nature of the material. On the other hand, the CS is an important factor which has to be taken into account before use of a material for a specific purpose. Permanent deformation, the compression set (CS) is an important parameter, particularly for the use of seals and shims made of elastomers. In order to determine this parameter a cylindrical test piece is compressed by e.g. 25% and stored thus for a certain time at a specific temperature. The temperature and the medium (usually air, but also oils and other industrial fluids) for the compression test depend on the material to be tested, its intended purpose and the test setup (e.g. 24 h at 150° C.). 30 minutes after decompression the height is again measured at room temperature and the permanent deformation ascertained therefrom. A compression set of 0% means that the test piece has again completely reached its original thickness; a CS of 100% indicates that the test piece has been completely deformed during the test and shows no resetting. The calculation is carried out according to the following formula: CS (%)=(L₀-L₂)/(L₀-L₁)×100%, wherein:

CS=compression set in %

L₀=height of the test piece before testing

L₁=height of the test piece during testing (spacer)

L₂=height of the test piece after testing.

In addition, the force in MPa according to DIN ISO 34-1, which is required to stretch the thermoplastic elastomer by 100%, 200% or 300%, was measured. Here a test piece—as defined in the named standard—is taken and stretched by the length indicated while measuring the force required.

Determination of the tear propagation resistance takes place according to DIN 53504/ISO 37.

The abrasion of the thermoplastic elastomer compositions is measured, by rubbing a 6 mm high cylinder with a diameter of 16 mm over 40 m of 60-grit sandpaper with a contact pressure of 10 N.

The adhesion of the thermoplastic elastomer compositions on polypropylene (type: Moplen® HP501L; manufacturer: Basell Polyolefins) is determined according to VDI2019.

Embodiment Examples

Table 1 indicates the abbreviations used for the components used in the examples:

TABLE 1 Component Raw material A Elastomer (rubber) B Non-elastomeric polyolefin C Thermoplastic elastomer based on polyolefin block copolymers D Cross-linking agent E Co-crosslinker F Plasticizer G Stabilizer, auxiliary material and dye H Filler

Examples 1 and 2 Production of Compositions of Thermoplastic Elastomers Based on EVM and NBR According to the Invention

According to the above-named production variant 3, a thermoplastic elastomer composition is produced with the constituents shown in Tables 2 and 3. A twin-screw extruder is used for blending the components used. The measured mechanical values are indicated in Table 4. Tables 5 to 7 indicate the mechanical values after treatment in various media.

TABLE 2 Compositions Raw material Component Example 1 Example 2 Elastomer (NBR) A1 100 Elastomer (EVM) A2 100 Non-elastomeric polyolefin B 20 16.7 TPO C 10 8.3 Cross-linker (10 wt. - % D 11 13.5 peroxide) Co-crosslinker E 6 6 Plasticizer F 25 25 Stabilization, auxiliary G materials and colour: Additive 1 0.46 0.4 Additive 2 0.24 0.24 Additive 3 0.24 0.25 Additive 4 0.2 0.2 Additive 5 0.1 Additive 6 1 Additive 7 1 Additive 8 1 Additive 9 3 3 Additive 10 1.5 3 Additive 11 0.3 0.4 Filler H 4 4

TABLE 3 Raw materials used Raw material Component Manufacturer Type Elastomer (NBR) A1 Lanxess Perbunan 3446 F Elastomer (EVM) A2 Lanxess EVM 600 Non-elastomeric polyolefin B Lyondell Basell Moplen HP500 N TPO C Lyondell Basell Hifax CA 10A Cross-linking agent D Pergan Peroxan HXY1OPSVP796 Co-crosslinker E Kettlitz PerTAC-GR Plasticizer F Safic Alkan Edenol T810T Stabilization, auxiliary G materials and colour: Additive 1 BASF Tinuvin 326 Additive 2 BASF Chimasorb 944 FDL Additive 3 BASF Tinuvin 622 SF Additive 4 BASF Irganox 1330 Additive 5 BASF Irganox 3052 FF Additive 6 Nordmann, Rassmann Quantox-45 Additive 7 Lanxess Vulkazon AFS-LG Additive 8 Rhein Chemie Antililux 654 Additive 9 Rhein Chemie Rhenogran PCD-50 EVA Additive 10 Lanxess Vulkanox HS LG Additive 11 BASF Irgafos 168 Fillers H Bayer ZnO Aktiv

TABLE 4 Mechanical values Value Unit Example 1 Example 2 Density g/cm³ 1.015 1.056 Hardness ShA 73 59 Tensile strength N/mm² 5.8 7.0 Elongation at break % 353 332 100% MPa 3.0 2.5 200% MPa 3.9 4.3 300% MPa 5.1 6.4 Tear propagation resistance N/mm² 20 15.3 Compression set at 25° C./22 h % 32.0 31.0 Compression set at 700° C./22 h % 34.0 31.0 Compression set at 100° C./22 h % 39.5 30.5 Compression set at 120° C./22 h % 49.5 35.5 Compression set at 140° C./22 h % 67.0 52.0 Compression set at 150° C./22 h % 76.0 59.5 Adhesion on PP N/mm² 6 6 Abrasion mm³ 422 317 The values for density, hardness, tensile strength, elongation at break, expansion (100%, 200%, 300%) and tear propagation resistance are recorded at room temperature.

TABLE 5 Measured Treatment Example Example value period Medium Temperature 1 2 Density Δ% Start value IRM 901 100° C. 0.0 0.0 1 week −3.5 2.2 3 weeks −0.2 3.6 Weight Δ% Start value 0.0 0.0 1 week −0.8 −4.6 3 weeks −1.7 −5.2 Volume Δ% Start value 0.0 0.0 1 week −4.3 −2.5 3 weeks −1.9 −1.8 Hardness Start value 73 60 (ShA) 1 week 76 60 3 weeks 73 59 Tensile Start value 6.6 6.8 strength 1 week 5.1 5.5 (N/mm²) 3 weeks 4.1 4.9 Elongation Start value 414 366 at break (%) 1 week 287 278 3 weeks 151 250 100 Start value 3.1 2.3 (MPa) 1 week 3.3 2.4 3 weeks 3.6 2.4 200% Start value 3.9 3.9 (MPa) 1 week 4.3 4.2 3 weeks 0.0 4.2 300% Start value 4.9 5.8 (MPa) 1 week 0.0 0.0 3 weeks 0.0 0.0

TABLE 6 Measured Treatment Example Example value period Medium Temperature 1 2 Density Δ% Start value Diesel RT 0.0 0.0 1 week 10.5 44.9 3 weeks 6.5 40.4 Weight Δ% Start value 0.0 0.0 1 week −2.6 −10.1 3 weeks −2.3 −9.7 Volume Δ% Start value 0.0 0.0 1 week 7.6 30.3 3 weeks 4.1 26.7 Hardness (ShA) Start value 73 60 1 week 65 41 3 weeks 68 42 Tensile strength Start value 6.6 6.8 (N/mm²) 1 week 4.6 2.6 3 weeks 5.0 2.7 Elongation at Start value 414 366 break (%) 1 week 341 191 3 weeks 347 192 100% (MPa) Start value 3.1 2.3 1 week 2.3 1.5 3 weeks 2.6 1.5 200% (MPa) Start value 3.9 3.9 1 week 3.2 0.0 3 weeks 3.4 0.0 300% (MPa) Start value 4.9 5.8 1 week 4.2 0.0 3 weeks 4.4 0.0

TABLE 7 Measured Treatment Example Example value period Medium Temperature 1 2 Density Δ% Start value Air 100° C. 0.0 0.0 1 week −1.5 3.0 3 weeks −1.5 3.5 6 weeks −2.0 3.6 Weight Δ% Start value 0.0 0.0 1 week 0.6 −3.4 3 weeks 0.5 −3.7 6 weeks 0.7 −4.1 Volume Δ% Start value 0.0 0.0 1 week −0.9 −0.4 3 weeks −1.0 −0.4 6 weeks −1.3 −0.6 Hardness (ShA) Start value 73 60 1 week 76 63 3 weeks 76 61 6 weeks 78 63 Tensile strength Start value 6.6 6.8 (N/mm²) 1 week 6.4 6.6 3 weeks 5.9 6.6 6 weeks 5.9 6.7 Elongation at Start value 414 366 break (%) 1 week 333 315 3 weeks 291 330 6 weeks 230 317

TABLE 8 Measured Treatment Example Example value period Medium Temperature 1 2 100% (MPa) Start value Air 100° C. 3.1 2.3 1 week 3.5 2.6 3 weeks 3.5 2.5 6 weeks 4.0 2.7 200% (MPa) Start value 3.9 3.9 1 week 4.6 4.6 3 weeks 4.7 4.3 6 weeks 5.5 4.6 300% (MPa) Start value 4.9 5.8 1 week 6.0 6.5 3 weeks 0.0 6.2 6 weeks 0.0 6.6

Examples 3 to 6 Production of Compositions of Thermoplastic Elastomers Based on SBR and NR According to the Invention

According to the above-named production variant 3, a thermoplastic elastomer composition is produced with the constituents shown in Tables 9 and 10. A twin-screw extruder is used for blending the components used.

Both TPEs based on SBR and TPEs based on NR result in homogeneous mixtures with good adhesion properties on polypropylene. As examples of this, the measured mechanical values and the values for the adhesion on polypropylene for TPEs based on SBR are indicated in Table 11.

TABLE 9 Raw material Component Example 3 Example 4 Example 5 Example 6 Elastomer (SBR) A1 100 100 Elastomer (NR) A2 100 100 Non-elastomeric polyolefin B 26.7 26.7 26.7 26.7 TPO C 13.3 13.3 13.3 13.3 Cross-linker D 10 10 10 10 Plasticizer F 40 40 40 40 Stabilization, auxiliary materials G and colour: Additive 1 0.3 0.3 0.3 0.3 Additive 2 0.1 0.1 0.1 0.1 Additive 3 0.32 0.32 0.32 0.32 Additive 4 0.1 0.1 0.1 0.1 Additive 5 8 8 Filler H 4 4 4 4

TABLE 10 Raw materials used Raw material Component Manufacturer Type Elastomer (SBR) A1 synthos Kralex SBR 1502 Elastomer (NR) A2 Weber & Schaer Natural Rubber SIR 20 Non-elastomeric polyolefin B Lyondell Basell Moplen HP500 N TPO C Lyondell Basell Hifax CA 10A Cross-linking agent (phenolic D SI Group SP 1045H resin) Plasticizer (white oil) F Shell Shell Ondina 941 Stabilization, auxiliary materials G and colour: Additive 1 BASF Tinuvin 326 Additive 2 BASF Chimasorb 944 FDL Additive 3 BASF Irganox 1330 Additive 4 BASF Irgafos 168 Additive 5 Rhenogran Zheolite 70 Rhein Chemie Additives Fillers H Bayer ZnO Aktiv

TABLE 11 Mechanical values Value Unit Example 3 Example 4 Density g/cm³ 0.927 0.94 Hardness ShA 64 64 Tensile strength N/mm² 4 4.1 Elongation at break % 209 206 100% MPa 2.5 2.7 200% MPa 4.0 4.1 Tear propagation resistance N/mm² 13.3 16.3 Compression set at 700° C./22 h % 26.5 25.0 Compression set at 1000° C./22 h % 33.3 30.5 Compression set at 1200° C./22 h % 46.0 47.0 Adhesion on PP N/mm² 4.5 4.7 The values for density, hardness, tensile strength, elongation at break, expansion (100%, 200%) and tear propagation resistance are recorded at room temperature. 

1. A thermoplastic elastomer composition comprising: an elastomer, a non-elastomeric polyolefin, and a thermoplastic elastomer based on polyolefin block copolymers (TPO), wherein the elastomer includes a first elastomer selected from the group consisting of ethylene-vinyl acetate copolymer, nitrile butadiene rubber, hydrogenated nitrile butadiene rubber, butyl rubber, natural rubber, isoprene rubber, acrylate rubber, ethylene acrylate rubber, silicone rubber, styrene butadiene rubber, chloroprene rubber, bromobutyl rubber, epichlorohydrin rubber, and epoxidized natural rubber, or a mixture thereof, and wherein the first elastomer is cross-linked or non-cross-linked.
 2. The thermoplastic elastomer composition according to claim 1, wherein the first elastomer is cross-linked.
 3. The thermoplastic elastomer composition according to claim 1, wherein the mixture of non-elastomeric polyolefin and TPO represents a matrix into which the elastomer is incorporated.
 4. The thermoplastic elastomer composition according to claim 1, wherein the TPO is a block copolymer which contains at least two different alkylene units.
 5. The thermoplastic elastomer composition according to claim 1, wherein the non-elastomeric polyolefin is a polypropylene.
 6. The thermoplastic elastomer composition according to claim 1, wherein a weight ratio of elastomer to non-elastomeric polyolefin lies in a range of from 100:15 to 100:60.
 7. The thermoplastic elastomer composition according to claim 1, wherein the weight ratio of elastomer to TPO lies in the range of from 100:5 to 100:45.
 8. A mixture of an elastomer and a cross-linking agent for the elastomer for producing the thermoplastic elastomer composition according to claim
 1. 9. A mixture of a non-elastomeric polyolefin and a TPO for producing the thermoplastic elastomer composition according to claim
 1. 10. The thermoplastic elastomer composition according to claim 1 for producing a composite material with a polyolefin.
 11. An article produced from the thermoplastic elastomer according to claim 1 and a polyolefin.
 12. The thermoplastic elastomer composition according to claim 1 for producing components or shaped bodies in automobile interiors or in the engine space of vehicles, for producing industrial devices, industrial tools, bathroom fittings, domestic appliances, consumer electronics devices, sporting goods, medical consumables and devices, containers for sanitary products and cosmetics, and sealing materials.
 13. A process for producing the thermoplastic elastomer composition according to claim 1, comprising: mixing the elastomer, the non-elastomeric polyolefin and the TPO.
 14. The process according to claim 13, wherein in a first step the first elastomer is pre-treated and in a second step the mixture of non-elastomeric polyolefin and TPO is added.
 15. The process according to claim 14, wherein in the first step the first elastomer is softened by a temperature effect and mixed with a cross-linking agent.
 16. The process according to claim 14, wherein before the second step the mixture of non-elastomeric polyolefin and TPO is produced in an extruder, an internal mixer or a kneader.
 17. The thermoplastic elastomer composition according to claim 5, wherein the polypropylene is hPP.
 18. The process according to claim 15, wherein the first elastomer is softened at a temperature in the range of from 50° C. to 120° C. and mixed with a cross-linking agent.
 19. The process according to claim 15, wherein the first elastomer is softened at a temperature in the range of from 80° C. to 110° C. and mixed with a cross-linking agent.
 20. The process according to claim 16, wherein before the second step the mixture of non-elastomeric polyolefin and TPO is produced in a twin-screw extruder. 